01 2Aurobindo Pharma Limited
02 1Chromo Laboratories India Private Limited
03 1Cipla Ltd.
04 1DISHMAN CARBOGEN AMCIS LIMITED
05 1Glaxo Operations UK Ltd
06 2Hetero Labs Limited
07 1MYLAN LABORATORIES LIMITED
08 1Olon SpA
09 1Piramal Pharma Limited
10 1ThermoFisher Scientific Cork
11 2Tianish Laboratories Private Limited
12 1Viyash Life Sciences Private Limited
01 4ABACAVIR SULFATE
02 8Abacavir Sulfate
03 1Abacavir Sulfate (Process II)
04 2abacavir sulfate
01 10India
02 1Italy
03 3U.S.A
04 1United Kingdom
NDC Package Code : 65862-256
Start Marketing Date : 2024-01-11
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 59651-946
Start Marketing Date : 2024-02-20
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (50kg/50kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 52562-036
Start Marketing Date : 2024-12-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 53104-7558
Start Marketing Date : 2018-04-05
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (25kg/25kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61876-0718
Start Marketing Date : 2013-07-15
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 63379-049
Start Marketing Date : 2014-08-04
End Marketing Date : 2026-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 17337-0001
Start Marketing Date : 2012-12-04
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65085-0024
Start Marketing Date : 2009-05-01
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (20kg/20kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 61187-010
Start Marketing Date : 2016-09-29
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
NDC Package Code : 65015-640
Start Marketing Date : 2015-02-13
End Marketing Date : 2025-12-31
Dosage Form (Strength) : POWDER (1kg/kg)
Marketing Category : BULK INGREDIENT
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PharmaCompass offers a list of Abacavir Sulfate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Abacavir Sulfate manufacturer or Abacavir Sulfate supplier for your needs.
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A ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE, including repackagers and relabelers. The FDA regulates ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE supplier is an individual or a company that provides ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE active pharmaceutical ingredient (API) or ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE finished formulations upon request. The ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE suppliers may include ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE API manufacturers, exporters, distributors and traders.
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National Drug Code is a comprehensive database maintained by the FDA that contains information on all drugs marketed in the US. This directory includes information about finished drug products, unfinished drug products, and compounded drug products, including those containing ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE as an active pharmaceutical ingredient (API).
The FDA updates the NDC directory daily. The NDC numbers for ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE API and other APIs are published in this directory by the FDA.
The NDC unfinished drugs database includes product listing information submitted for all unfinished drugs, such as active pharmaceutical ingredients (APIs), drugs intended for further processing and bulk drug substances for compounding.
Pharmaceutical companies that manufacture ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE as an active pharmaceutical ingredient (API) must furnish the FDA with an updated record of all drugs that they produce, prepare, propagate, compound, or process for commercial distribution in the US at their facilities.
The NDC directory also contains data on finished compounded human drug products that contain ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE and are produced by outsourcing facilities. While these outsourcing facilities are not mandated to assign a ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE NDC to their finished compounded human drug products, they may choose to do so.
click here to find a list of ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE suppliers with NDC on PharmaCompass.
We have 12 companies offering ABACAVIR SULFATE, LAMIVUDINE AND ZIDOVUDINE
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